Evidence map›Paper›PMID 38153767›Full record

ArticleDNA research : an international journal for rapid publication of reports on genes and genomes2024

ZSCAN4-binding motif-TGCACAC is conserved and enriched in CA/TG microsatellites in both mouse and human genomes.

Tomohiko Akiyama, Kei-Ichiro Ishiguro, Nana Chikazawa, Shigeru B H Ko, Masashi Yukawa, Minoru S H Ko

Open access · goldAbstract read
In one paragraph

Article in DNA research : an international journal for rapid publication of reports on genes and genomes, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.2field-weighted citation impact, top 20% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Reprogramming Chromosome Ends by Functional Histone Acetylation.International journal of molecular sciences · 2024
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 2 countries.

Tomohiko AkiyamaDepartment of Systems Medicine, Keio University School of Medicine, Tokyo 160-8582, Japan.
Kei-Ichiro IshiguroDepartment of Systems Medicine, Keio University School of Medicine, Tokyo 160-8582, Japan.ORCID 0000-0002-7515-1511
Nana ChikazawaDepartment of Systems Medicine, Keio University School of Medicine, Tokyo 160-8582, Japan.
Shigeru B H KoDepartment of Systems Medicine, Keio University School of Medicine, Tokyo 160-8582, Japan.
Masashi YukawaIntegrated Medical and Agricultural School of Public Health, Ehime University, Ehime 791-0295, Japan.
Minoru S H KoDepartment of Systems Medicine, Keio University School of Medicine, Tokyo 160-8582, Japan.ORCID 0000-0002-3530-3015
Keio University · JPCincinnati Children's Hospital Medical Center · US

Funding

Japan Society for the Promotion of Science 17H01433
6 · The paper itself

Abstract

The Zinc finger and SCAN domain containing 4 (ZSCAN4) protein, expressed transiently in pluripotent stem cells, gametes, and early embryos, extends telomeres, enhances genome stability, and improves karyotypes in mouse embryonic stem (mES) cells. To gain insights into the mechanism of ZSCAN4 function, we identified genome-wide binding sites of endogenous ZSCAN4 protein using ChIP-seq technology in mouse and human ES cells, where the expression of endogenous ZSCAN4 was induced by treating cells with retinoic acids or by overexpressing DUX4. We revealed that both mouse and human ZSCAN4 bind to the TGCACAC motif located in CA/TG microsatellite repeats, which are known to form unstable left-handed duplexes called Z-DNA that can induce double-strand DNA breaks and mutations. These ZSCAN4 binding sites are mostly located in intergenic and intronic regions of the genomes. By generating ZSCAN4 knockout in human ES cells, we showed that ZSCAN4 does not seem to be involved in transcriptional regulation. We also found that ectopic expression of mouse ZSCAN4 enhances the suppression of chromatin at ZSCAN4-binding sites. These results together suggest that some of the ZSCAN4 functions are mediated by binding to the error-prone regions in mouse and human genomes.

Indexed as

Genome, HumanTranscription FactorsAnimalsDNA-Binding ProteinsGene Expression RegulationHumansMiceMicrosatellite RepeatsZinc FingersDNA-Binding ProteinsTranscription FactorsZSCAN4 protein, humanCA/TG microsatellitegenome stabilityhuman ES cellsmouse ES cellsZSCAN4

Identifiers

PMID38153767
PMCPMC10785592
OpenAlexW4390335240

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.